chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102063768820637689AC64GENIChomozygous116509648
102063800020638001CA67GENICpossibly homozygous116509650
102063839320638394CT69GENICheterozygous116509652
102064051820640519GA43GENICpossibly homozygous116509654
102064065020640651GA43GENIChomozygous116509656
102064142720641428TC49GENIChomozygous116509658
102064228320642284GA30GENIChomozygous116509660
102064229520642296CG32GENIChomozygous116509662
102064231520642316GA37GENIChomozygous116509664
102064235720642358GA39GENIChomozygous116509666
102064283920642840CT68GENIChomozygous116509668
102064293620642937CG69GENIChomozygous116509670
102064433820644339GC64GENIChomozygous116509672
102064457420644575CA71GENIChomozygous116509674
102064597220645973CT86GENIChomozygous116509676
102064661020646611TC22GENIChomozygous116509678
102064675620646757AG39GENIChomozygous116509680
102064710320647104CG56GENIChomozygous116509682
102064712120647122AG53GENIChomozygous116509684
102064743620647437AG56GENIChomozygous116509686
102064833220648333TC53GENICpossibly homozygous117983739
102064846120648462CG46GENIChomozygous116741582
102064928420649285GA46GENIChomozygous116509688
102064991420649915CT64GENIChomozygous116509690
102065123420651235CT59GENIChomozygous116509692
102065294920652950CT43GENIChomozygous116509694
102065304920653050AG57GENICpossibly homozygous116509696
102065305820653059CT55GENIChomozygous116509698
102065407120654072CT65GENIChomozygous116509700
102065525420655255GA60GENIChomozygous116509702
102065626120656262GC47GENIChomozygous116509706
102065722320657224CT73GENIChomozygous116509708
102065759920657600AG62GENIChomozygous116509710